direct lysis of cell pellet - How to get rid of DNA? (Jul/15/2010 )
I tried to directly lyse my cell pellets in a buffer containing 8M urea by incubating at RT for 1h. But when I tried to load my samples on SDS-PAGE, the solution was far too sticky. In my opinion this is due to DNA.
I have already tried centrifugation to pellet the DNA and passing the solution through a needle and both did not work. I do not want to heat my samples because of the urea. Any additional ideas how to get rid of the DNA?
Thanks in advance
firstly, y cant u heat becos of the urea?
have u tried using QIAgen shredder? It will help to get rid of the DNA but its kinda time-consuming though..
ursae on Jul 18 2010, 09:50 PM said:
urea will decompose and carbamylate the protein.
try sonication. 30s.